Primary Device ID | 04052199273662 |
NIH Device Record Key | 33aded43-0fae-4f4f-bf07-bffd9cd1c24e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HydroTac transp. comf. 10x20cm st P10 |
Version Model Number | 685927 |
Company DUNS | 315768788 |
Company Name | PAUL HARTMANN AG |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04052199273648 [Primary] |
GS1 | 04052199273655 [Package] Contains: 04052199273648 Package: [10 Units] In Commercial Distribution |
GS1 | 04052199273662 [Package] Contains: 04052199273655 Package: [4 Units] In Commercial Distribution |
NAD | Dressing, Wound, Occlusive |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-09-09 |
Device Publish Date | 2020-09-01 |
04052199273662 | HydroTac transp. comf. 10x20cm st P10 |
04049500835107 | HydroTac transp. comf. 10x20cm st P10 |